Variant #0001925880 (NC_000022.10:g.37868526A>T, NM_002405.3:c.854T>A (MFNG))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37868526A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MFNG_000014
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 08:09:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MFNG NM_002405.3 ?/? c.854T>A r.(?) p.(Val285Asp)